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Neonatal lethality, dwarfism, and abnormal brain development in Dmbx1 mutant mice
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
title
Neonatal lethality, dwarfism, and abnormal brain development in Dmbx1 mutant mice
(English)
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
main subject
brain
0 references
Diencephalon/mesencephalon homeobox 1
1 reference
stated in
GOA release 2020-03-11
author
Richard R. Behringer
series ordinal
2
object named as
Richard R. Behringer
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
author name string
Akihira Ohtoshi
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 September 2004
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
published in
Molecular and Cellular Biology
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
volume
24
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
issue
17
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stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
page(s)
7548–7558
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stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
cites work
The homeobox gene mbx is involved in eye and tectum development
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Regionalisation of anterior neuroectoderm and its competence in responding to forebrain and midbrain inducing activities depend on mutual antagonism between OTX2 and GBX2
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17 March 2017
Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development
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PubMed Central
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17 March 2017
The winged helix gene, Foxb1, controls development of mammary glands and regions of the CNS that regulate the milk-ejection reflex
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PubMed Central
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17 March 2017
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
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PubMed Central
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Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a
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Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome
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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain
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Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development
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Protamine-Cre recombinase transgenes efficiently recombine target sequences in the male germ line of mice, but not in embryonic stem cells
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Lactation defect in mice lacking the helix-loop-helix inhibitor Id2
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Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets
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29 September 2017
A mouse model for achondroplasia produced by targeting fibroblast growth factor receptor 3.
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29 September 2017
Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function
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Oxytocin is required for nursing but is not essential for parturition or reproductive behavior
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A defect in nurturing in mice lacking the immediate early gene fosB.
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29 September 2017
The embryonic vertebrate forebrain: the prosomeric model.
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29 September 2017
Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum
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29 September 2017
The paired-type homeobox gene Dmbx1 marks the midbrain and pretectum.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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3 June 2018
Isolation and characterization of Vsx1, a novel mouse CVC paired-like homeobox gene expressed during embryogenesis and in the retina
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PubMed Central
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3 June 2018
Homeobox genes in the developing mouse brain.
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PubMed Central
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Regionalization of the prosencephalic neural plate.
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3 June 2018
Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LH.
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PubMed Central
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3 June 2018
TWH regulates the development of subsets of spinal cord neurons.
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PubMed Central
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3 June 2018
Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism
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3 June 2018
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3 June 2018
Dmbx1 is a paired-box containing gene specifically expressed in the caudal most brain structures.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Dmbx1, a novel evolutionarily conserved paired-like homeobox gene expressed in the brain of mouse embryos.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Regulation of maternal behavior and offspring growth by paternally expressed Peg3.
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PubMed Central
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27 November 2018
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Fkh5-deficient mice show dysgenesis in the caudal midbrain and hypothalamic mammillary body.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Mouse Otx2 functions in the formation and patterning of rostral head.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Forebrain and midbrain regions are deleted in Otx2−/− mutants due to a defective anterior neuroectoderm specification during gastrulation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
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27 November 2018
Targeted disruption of the pituitary glycoprotein hormone alpha-subunit produces hypogonadal and hypothyroid mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507007
retrieved
27 November 2018
A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15314164
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1128/MCB.24.17.7548-7558.2004
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
PMCID
507007
0 references
PubMed ID
15314164
1 reference
stated in
PubMed
PubMed ID
15314164
retrieved
31 January 2017
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